Regulation of microRNA-1 (miR-1) expression in human cancer

被引:39
作者
Han, Chao [1 ,2 ]
Shen, Jacson K. [2 ]
Hornicek, Francis J. [2 ]
Kan, Quancheng [1 ]
Duan, Zhenfeng [1 ,2 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Pharm, 1 Jianshe East Rd, Zhengzhou 450052, Peoples R China
[2] Massachusetts Gen Hosp, Ctr Sarcoma & Connect Tasue Oncol, Sarcoma Biol Lab, 100 Blossom St,Jackson 1115, Boston, MA 02114 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2017年 / 1860卷 / 02期
基金
中国国家自然科学基金;
关键词
miRNA; miR-1; Cancer; Regulatory mechanisms; ACUTE MYELOID-LEUKEMIA; LONG NONCODING RNA; DNA METHYLATION; DOWN-REGULATION; TUMOR-SUPPRESSOR; GENE-EXPRESSION; MIRNA; MIGRATION; INVASION; DYSREGULATION;
D O I
10.1016/j.bbagrm.2016.12.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRs) have been found to play important roles in tumorigenesis, apoptosis, metastasis, and drug resistance in cancer. Among a number of miRs, miR-1 was shown to be predominantly downregulated in almost all examined human cancers. As a tumor suppressor miR involved in post-transcriptional regulation of crucial tumor associated gene expression, miR-1 represents a promising target for anticancer therapy. Re-expression of miR-1 can suppress cancer cell proliferation, promote apoptosis, and reverse drug resistance in cancers both in vitro and in vivo. Recently, the regulatory mechanisms of miR-1 expression have been studied in various cancers in different model systems. In this review, we summarize the mechanisms of miR-1 expression through epigenetic, transcriptional, and post-transcriptional regulation. These regulatory mechanisms of miR-1 expression could help us to understand the functions of altered miR-1 expression and provide valuable insights for further investigations into miR-1 based cancer therapy. Published by Elsevier B.V.
引用
收藏
页码:227 / 232
页数:6
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